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首页> 外文期刊>Journal of Photochemistry and Photobiology, A. Chemistry >Surface-enhanced Raman scattering at well-defined single crystalline faces of platinum-group metals induced by gap-mode plasmon excitation
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Surface-enhanced Raman scattering at well-defined single crystalline faces of platinum-group metals induced by gap-mode plasmon excitation

机译:间隙模式等离子体激元激发在铂族金属的明确单晶面上的表面增强拉曼散射

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摘要

It is normally difficult to use surface enhanced Raman scattering (SERS) to study molecular adsorbates at well-defined planar metal surfaces or at Pt-group catalytic metal surfaces. In this paper, highly localized gap-mode plasmons are excited on atomically smooth metal surfaces by using a sphere-plane type plasmonic cavity. This method enables us to observe Raman scattering signals from molecular adsorbates on various single crystalline metal surfaces including non-SERS-active Pt and Pd. SERS spectra of self-assembled isocyanide monolayers on several metal substrates with (111) or (100) orientation reveal a significant orientation dependence of preferential adsorption sites, which information is hardly obtainable from conventional SERS spectra.
机译:通常很难使用表面增强拉曼散射(SERS)来研究轮廓分明的平面金属表面或Pt基催化金属表面的分子吸附物。在本文中,通过使用球面型等离子体激元腔,在原子光滑的金属表面上激发了高度局限的间隙模等离子体激元。这种方法使我们能够观察到来自包括非SERS活性Pt和Pd在内的各种单晶金属表面上分子吸附物的拉曼散射信号。具有(111)或(100)取向的几种金属基材上的自组装异氰酸酯单层的SERS光谱显示优先吸附位的显着取向依赖性,该信息很难从常规SERS光谱中获得。

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